Job Description SummaryThis role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods and current Compendia.Key ResponsibilitiesExecutes analyses on excipients, raw materials, finished products and packaging per internal SOPs and applicable pharmacopeias.Conducts stability studies, process and method validations, and activities related to technology transfer of pharmaceutical products.Performs instrument qualification and re-qualification (IQ/OQ/PQ) according to internal procedures.Records analytical data in compliance with ALCOA principles and data integrity requirements.Reviews GMP documentation, batch records, analytical reports and certificates for completeness and compliance.Collaborates with QA, Production and R&D; supports method transfers, troubleshooting and safe lab/5S practices.Participates in audits and inspections by providing data and responses; contributes to CAPA, deviations, change control and SOP updates.Tracks KPIs: on‑time completion and right‑first‑time rates, data integrity compliance, audit outcomes, documentation quality and continuous improvement impact.Essential RequirementsDegree in Chemistry.Solid technical-scientific knowledge of pharmaceutical/chemical QC or equivalent analysis.Previous experience working in a laboratory environment in the pharmaceutical industry.Experience in a GMP environment.Fluent in Italian and English.Why NovartisOur purpose is to reimagine medicine to improve and extend people’s lives. Join us to help achieve this mission. Learn more about our benefits and rewards in Novartis Life.Diversity and InclusionNovartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.Employment TypeFull‑TimeExperienceYears of experience required: years.Vacancy1
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